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Brand-name prescription medicine

Norgesic

Generic name: Orphenadrine citrate, aspirin and caffeine

FDA application holder: Galt Pharms

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Norgesic?
Norgesic is a brand name of Orphenadrine citrate, aspirin and caffeine, a prescription medicine. The FDA NDC Directory lists 1 Norgesic product in 1 strength and form.
Who makes Norgesic?
Galt Pharms holds the FDA application for Norgesic (ANDA075141, approved May 29, 1998).
Is there a generic or store brand of Norgesic?
Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Norgesic product, 1 of them generic. Ask your pharmacist whether one is right for you.
Has Norgesic been recalled?
No recall linked to Norgesic products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Norgesic is

Each Norgesic product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Orphenadrine citrate, aspirin and caffeine · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
aspirin 385 mg · caffeine 30 mg · orphenadrine citrate 25 mg
tablet (oral)
Norgesic 1 product, 1 company DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Orphenadrine citrate, aspirin and caffeine →

FDA approval

  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
FDA applications of Norgesic products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
ANDA075141Galt PharmsMay 29, 19981

Companies that list Norgesic

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Norgesic products.

Recalls

No recall linked to Norgesic products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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